当前位置:易推广 > 上海陶术生物科技有限公司 > 产品展示
企业档案
会员类型:会员
已获得易推广信誉 等级评定
(0 -40)基础信誉积累,可浏览访问
(41-90)良好信誉积累,可接洽商谈
(91+ )优质信誉积累,可持续信赖
易推广会员:5年
最后认证时间:
注册号: 【已认证】
法人代表: 【已认证】
企业类型:生产商 【已认证】
注册资金:人民币万 【已认证】
产品数:86101
参观次数:3809891
已选条件
-
T27834Limonin glucoside;化合物 T27834CCRIS-6986|||CCRIS 6986|||CCRIS6986;CCRIS-6986|||CCRIS 6986|||CCRIS6986
Limonin glucoside is a natural product in citrus fruits. It inhibits expression of HIV-1 and HTLV-1 in infected cells, induces apoptosis in colon adenocarcinoma cells, and exhibits larvicidal activity against species of Aedes.
价 格:¥电议型 号:T27834产 地:中国大陆
-
T27717KCC009;化合物 T27717KCC-009|||KCC 009;KCC-009|||KCC 009
KCC009 is a potent and selective Transglutaminase 2 Inhibitor.
价 格:¥电议型 号:T27717产 地:中国大陆
-
T27682CCR2 antagonist 5;化合物CCR2 antagonist 5JNJ-41443532|||JNJ-41443532 Free Base|||JNJ 41443532|||JNJ4144
CCR2 antagonist 5 (JNJ-41443532) is a selective and orally active hCCR2 inhibitor with good binding affinity (IC50=37 nM) and potent functional antagonism (chemotaxis IC50=30 nM).JNJ-41443532 binds mCCR2 with a Ki of 9.6 ?M, which can be used to study inflammatory diseases and diabetes. diseases and diabetes.
价 格:¥电议型 号:T27682产 地:中国大陆
-
T27579ICL-CCIC-0019;化合物ICL-CCIC-0019ICL CCIC 0019;ICL CCIC 0019
ICL-CCIC-0019 is an inhibitor of choline kinase alpha (ChoKα). ICL-CCIC-0019 induces G1 arrest, endoplasmic reticulum stress, and apoptosis of cancer cell lines.
价 格:¥电议型 号:T27579产 地:中国大陆
-
T27332Flestolol sulfate;化合物 T27332ACC 9089|||ACC-9089|||ACC9089;ACC 9089|||ACC-9089|||ACC9089
Flestolol sulfate is an anti-adrenergic beta-receptor.
价 格:¥电议型 号:T27332产 地:中国大陆
-
T27286LEsprolol;化合物 EsprololACC-9369 free base;ACC-9369 free base
Esprolol (ACC-9369 free base) is a novel β-adrenergic receptor antagonist for the study of exertional angina.
价 格:¥电议型 号:T27286L产 地:中国大陆
-
T27286Esprolol hydrochloride;化合物 T27286ACC9369|||ACC 9369|||ACC-9369;ACC9369|||ACC 9369|||ACC-9369
Esprolol is a β-adrenergic receptor antagonist.
价 格:¥电议型 号:T27286产 地:中国大陆
-
T27283Erysolin;化合物 T27283CCG-38863|||CCG 38863|||ACM-504847|||ACM 504847|||CCG38863|||ACM504847;CCG-38863|
Erysolin, a sulforaphane analog found in cruciferous vegetables, induces phase II enzyme activity and inhibits growth of colon cancer cells.
价 格:¥电议型 号:T27283产 地:中国大陆
-
T27282Erucin;化合物 T27282AR 1G3839|||AR-1G3839|||CCRIS-9056|||CCRIS9056|||AR1G3839|||CCRIS 9056;AR 1G3839|||
Erucin is a sulforaphane analog found in cruciferous vegtables. Erucin is a telomerase inhibitor. It induces phase II enzyme activity, suppresses cellular proliferation in hepatocellular carcinoma cells, prevents 6-OHDA-induced neurodegenration, and inhibits LPS-stimulated pro inflammatory cytokine expression in vivo.
价 格:¥电议型 号:T27282产 地:中国大陆
-
T2719Succinic acid琥珀酸Asuccin|||Amber acid|||琥珀酸|||1,2-Ethanedicarboxylic acid|||Wormwood acid|||Butanedio
Succinic acid (1,2-Ethanedicarboxylic acid) is a water-soluble, colorless crystal with an acid taste that is used as a chemical intermediate, in medicine, the manufacture of lacquers, and to make perfume esters. It is also used in foods as a sequestrant, buffer, and a neutralizing agent.
价 格:¥电议型 号:T2719产 地:中国大陆
-
T26969CCT365623;化合物CCT365623CCT-365623|||CCT 365623;CCT-365623|||CCT 365623
CCT365623 is an orally bioavailable Lysyl Oxidase inhibitor with good anti-LOX potency, selectivity, pharmacokinetic properties, as well as anti-metastatic efficacy.
价 格:¥电议型 号:T26969产 地:中国大陆
-
T26968CCT036477;化合物 T26968CCT 036477|||CCT-036477;CCT 036477|||CCT-036477
CCT036477 is a selective inhibitor of wingless-type MMTV integration site family dependent transcription. CCT036477reduces the transcriptional activity of the T-cell factor and lymphoid enhancer factor transcription factor family at the ?-catenin level.
价 格:¥电议型 号:T26968产 地:中国大陆
-
T26967CCG-232601;化合物 T26967CCG 232601|||CCG232601;CCG 232601|||CCG232601
CCG-232601 is a inhibitor of the Rho/MRTF/SRF transcriptional pathway.
价 格:¥电议型 号:T26967产 地:中国大陆
-
T26966CCD-3693;化合物 T26966CCD 3693|||CO32693|||CO 32693|||CO-32693|||CCD3693;CCD 3693|||CO32693|||CO 32693|
CCD-3693 is a gamma-aminobutyric acid (GABA) receptor agonist.
价 格:¥电议型 号:T26966产 地:中国大陆
-
T26965CC34301;化合物 T26965CC-34301|||CC 34301;CC-34301|||CC 34301
CC34301, a PqsE inhibitor, binds to the active center of PqsE, inhibiting its thioesterase activity in cell-based and in vitro assays.
价 格:¥电议型 号:T26965产 地:中国大陆
-
T26688Avadomide HCl;化合物 T26688Avadomide hydrochloride|||CC122, Avadomide HCl|||CC-122|||CC 122 HCl;Avadomi
Avadomide is an orally available pleiotropic pathway modulator with potential antineoplastic activity. CC-122 mimics an interferon response and has antitumor activity in DLBCL CC-122 binds Cereblon (CRBN) and promotes degradation of Ikaros and Aiolos in diffuse large B-cell lymphoma (DLBCL) and T cells in vitro, in vivo, and in patients, resulting in both cell autonomous as well as immunostimulatory effects.
价 格:¥电议型 号:T26688产 地:中国大陆
-
T2640Rebastinib;化合物DCC-2036DCC2036|||DCC 2036|||DCC-2036;DCC2036|||DCC 2036|||DCC-2036
DCC-2036 (Rebastinib (DCC-2036)) is a conformational control Bcr-Abl inhibitor for Abl1(WT, IC50: 0.8 nM) and Abl1(T315I, IC50: 4 nM), also inhibits LYN, SRC, HCK, FGR, FLT3, KDR, and Tie-2, and low activity to c-Kit. Rebastinib aimed at the Angiopoietin2-Tie2 pathway.
价 格:¥电议型 号:T2640产 地:中国大陆
-
T26267PHCCC(4Me);化合物 T26267THCCC;THCCC
THCCC, a PHCCC analog, is a dual metabotropic glutamate receptor 2/3 negative/positive allosteric modulator.
价 格:¥电议型 号:T26267产 地:中国大陆
-
T26197Snf 8815;化合物 T26197Snf8815|||Snf-8815|||28-Mephe-31-N-meile-cck (26-33);Snf8815|||Snf-8815|||28-Meph
Snf 8815 is an antagonist of cholecystokinin-B (CCK-B).
价 格:¥电议型 号:T26197产 地:中国大陆
-
T2611CCT 137690;化合物CCT137690CCT137690;CCT137690
CCT 137690 is a highly specific and oral-available aurora kinase inhibitor, for aurora A(IC50=15 nM ), B(IC50=25 nM) and C(IC50=19 nM).
价 格:¥电议型 号:T2611产 地:中国大陆